A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv470878



Internal ID15385706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22573382..22613047hg38UCSC Ensembl
Innerchr22:22915822..22955517hg19UCSC Ensembl
Innerchr22:21245822..21285517hg18UCSC Ensembl
Innerchr22:21240376..21280071hg16UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg3839666
hg1939696
hg1839696
hg1639696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv438338
Supporting Variants
SamplesNA18526
Known Genes
MethodSNP array
AnalysisNull genotypes - for each genotype assay and population sample we defined the null genotype pattern of that assay as the binary vector (length 90) of null genotype calls across the 90 individuals.
PlatformNot reported
Comments
ReferenceMcCarroll_et_al_2006
Pubmed ID16468122
Accession Number(s)nssv470878
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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